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Morepen Labs Baddi facility clears USFDA inspection without any adverse observation
Gurugram: Morepen Labs has recently announced that the United States Food and Drug Administration (USFDA) has conducted an inspection of the API manufacturing facility, at Baddi, Himachal Pradesh, of the company.
"The facility has been cleared by USFDA on 24th March 2023 without any adverse observation (NIL 483)," the company stated in a BSE filing.
Read also: Morepen Labs forms new subsidiary for medical devices
Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751